Obesity
Conditions
Interventions
05 men (Group 1) were overweight or obese at first receiving a biscuit containing 10 g / day of ora-pro-nobis meal. E 04 men (Group 2) received another biscuit, containing all the ingredients of the f
Other
Sponsors
Universidade Federal de Alfenas
Universidade Federal de Alfenas
Eligibility
Sex/Gender
Male
Age
No minimum to 59 Years
Inclusion criteria
Inclusion criteria: Men between the ages of 20 and 50; Body mass index greater than or equal to 25 kg / m² and less than 40 kg / m²; Not having participated in a weight loss program in the last six months; Be healthy
Exclusion criteria
Exclusion criteria: History of alcohol or drug abuse; diagnoses of cardiac, renal, gastrointestinal, hepatic, pulmonary, neurological, psychiatric, hematological or metabolic pathologies; restrictive diet practices
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Reduction of gastrointestinal symptoms, assessed using the symptom rating scale questionnaire of at least 5 points of the total score, made 1 week pre and post intervention.;Expected outcome 2: Reduction of total cholesterol and fractions, assessed by laboratory tests performed 1 week pre and post intervention.;Expected outcome 3: Reduced fasting blood glucose, assessed by laboratory tests performed 1 week pre and post intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Outcome found 1: There was reduction of gastrointestinal symptoms of at least 5 points of the total score, assessed by the symptom rating scale questionnaire made 1 week pre and post intervention.;Outcome Found 2:There was no reduction in total cholesterol and fractions, assessed by laboratory tests performed 1 week pre and post intervention.;Outcome Found 3: There was no reduction in fasting blood glucose, assessed by laboratory tests performed 1 week pre and post intervention. | — |
Countries
Brazil
Contacts
Public ContactRoberta Silva
Universidade Federal de Alfenas
Outcome results
None listed